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Dissipative soliton molecules (DSMs) are of great interest for studying the complexity of nonlinear optical problems as they can map with the matter molecules for making interdisciplinary analogies. In contrast to strongly bound DSMs that have a short time separation between the bound solitons, the complex dynamics and underlying binding mechanism of loosely bound soliton molecules (LBSMs) with orders of magnitude longer time separation remain open questions. To this end, here, we explore real-time spectroscopy using a dispersive temporal interferometer (DTI) to visualize the dynamics of LBSMs in a mode-locked fiber laser and unveil their underlying phase-evolving mechanism. The DTI enables fringe-resolved spectroscopy in real time of the LBSM’s evolution by creating duplicates of the LBSM that results in a much closer time separation between the individual solitons of the LBSM. The real-time evolution of the LBSM’s phase exhibits a diverging sliding landscape, which is theoretically and experimentally proved to be closely associated with gain dynamics. Based on the understanding of its phase dynamics, we finally demonstrate programmable phase-encoding modulation of the LBSM through gain control. These efforts not only shed light on understanding the mechanism of long-range interactions in LBSMs but also provide an alternative approach for all-optical information processing.

Bi2Te3-based materials have been reported to be one of the best room-temperature thermoelectric materials, and it is a challenge to substantially improve their thermoelectric properties. Here novel Bi2Te3 core fibers with borosilicate glass cladding were fabricated utilizing a modified molten core drawing method. The Bi2Te3 core of the fiber was found to consist of hexagonal polycrystalline nanosheets, and polycrystalline nanosheets had a preferential orientation; in other words, the hexagonal Bi2Te3 lamellar cleavage more tended to be parallel to the symmetry axis of the fibers. Compared with a homemade 3-mm-diameter Bi2Te3 rod, the polycrystalline nanosheets’ preferential orientation in the 89-μm-diameter Bi2Te3 core increased its electrical conductivity, but deduced its Seebeck coefficient. The Bi2Te3 core exhibits an ultrahigh ZT of 0.73 at 300 K, which is 232% higher than that of the Bi2Te3 rod. The demonstration of fibers with oriented nano-polycrystalline core and the integration with an efficient fabrication technique will pave the way for the fabrication of high-performance thermoelectric fibers.